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Alliance of Genome Resources

Alliance of Genome Resources is a gene dataset, which contains curated genome information essential for the understanding of the genetics and genomic basis of human biology, health and disease. All data is retrieved from six major model organism databases and the Gene Ontology including FlyBase, Mouse Genome Database (MGI), Rat Genome Database (RGD), Saccharomyces Genome Database (SGD), WormBase, Zebrafish Information Network (ZFIN), and the GO Consortium. In GlyCosmos, only glycan-related disease information has been extracted from Alliance of Genome Resources.

Source Last Updated
Alliance of Genome Resources October 9, 2024
Displaying entries 65351 - 65375 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID ▼ Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:10286 prostate carcinoma HGNC:11246 Homo sapiens (human) 6692 SPINT1
  • PMID:16492908
DOID:10652 Alzheimer's disease HGNC:11246 Homo sapiens (human) 6692 SPINT1
  • PMID:9743567
DOID:5517 stomach carcinoma HGNC:11246 Homo sapiens (human) 6692 SPINT1
  • PMID:16273651
DOID:1612 breast cancer HGNC:11246 Homo sapiens (human) 6692 SPINT1
  • PMID:14734471
DOID:5082 liver cirrhosis HGNC:11246 Homo sapiens (human) 6692 SPINT1
  • MGI:6194238
DOID:8893 psoriasis HGNC:11246 Homo sapiens (human) 6692 SPINT1
  • MGI:6194238
DOID:2394 ovarian cancer HGNC:11246 Homo sapiens (human) 6692 SPINT1
  • PMID:11948120
DOID:299 adenocarcinoma HGNC:11240 Homo sapiens (human) 8877 SPHK1
  • MGI:6194238
DOID:0050700 cardiomyopathy HGNC:11240 Homo sapiens (human) 8877 SPHK1
  • MGI:6194238
DOID:3070 high grade glioma HGNC:11240 Homo sapiens (human) 8877 SPHK1
  • MGI:6194238
DOID:9970 obesity HGNC:11240 Homo sapiens (human) 8877 SPHK1
  • MGI:6194238
DOID:9352 type 2 diabetes mellitus HGNC:11240 Homo sapiens (human) 8877 SPHK1
  • PMID:17265031
DOID:0110816 hereditary spastic paraplegia 7 HGNC:11237 Homo sapiens (human) 6687 SPG7
  • MGI:6194238
  • RGD:7240710
DOID:0110792 hereditary spastic paraplegia 4 HGNC:11233 Homo sapiens (human) 6683 SPAST
  • MGI:6194238
  • RGD:7240710
DOID:2476 hereditary spastic paraplegia HGNC:11233 Homo sapiens (human) 6683 SPAST
  • MGI:6194238
DOID:0110176 Charcot-Marie-Tooth disease axonal type 2X HGNC:11226 Homo sapiens (human) 80208 SPG11
  • RGD:7240710
DOID:0110764 hereditary spastic paraplegia 11 HGNC:11226 Homo sapiens (human) 80208 SPG11
  • MGI:6194238
  • RGD:7240710
DOID:0060197 amyotrophic lateral sclerosis type 5 HGNC:11226 Homo sapiens (human) 80208 SPG11
  • RGD:7240710
DOID:0050700 cardiomyopathy HGNC:11220 Homo sapiens (human) 8404 SPARCL1
  • MGI:6194238
DOID:856 biotinidase deficiency HGNC:1122 Homo sapiens (human) 686 BTD
  • MGI:6194238
  • RGD:7240710
DOID:0110338 osteogenesis imperfecta type 17 HGNC:11219 Homo sapiens (human) 6678 SPARC
  • RGD:7240710
DOID:5517 stomach carcinoma HGNC:11219 Homo sapiens (human) 6678 SPARC
  • MGI:6194238
DOID:2871 endometrial carcinoma HGNC:11219 Homo sapiens (human) 6678 SPARC
  • PMID:17487382
DOID:2152 ovary epithelial cancer HGNC:11219 Homo sapiens (human) 6678 SPARC
  • PMID:10502421
DOID:11713 diabetic angiopathy HGNC:11219 Homo sapiens (human) 6678 SPARC
  • MGI:6194238

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GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: December 9, 2024